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PRCD
Progressive rod-cone degeneration is a protein in humans that is encoded by the PRCD gene. 〔 (【引用サイトリンク】 url = http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=retrieve&list_uids=768206 )〕 This gene is predominantly expressed in the retina, and mutations in this gene are the cause of autosomal recessive retinal degeneration in both humans and dogs. Alternatively spliced transcript variants have been found for this gene. (by RefSeq, Mar 2010 ). == References ==
抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)』 ■ウィキペディアで「PRCD」の詳細全文を読む
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